Canonical Allele Identifier: CA477582339

Gene: SNX19

Linked Data

• gnomAD v4: 11-130880770-T-A
• MyVariant Identifiers: chr11:g.130750665T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880770T>A , CM000673.2:g.130880770T>A	GRCh38
NC_000011.9:g.130750665T>A , CM000673.1:g.130750665T>A	GRCh37
NC_000011.8:g.130255875T>A	NCBI36
NG_053190.1:g.40719A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2610A>T MANE Select	ENSP00000265909.4:p.Pro870=
ENST00000265909.8:c.2610A>T	ENSP00000265909.4:p.Pro870=
ENST00000426933.6:c.114A>T	ENSP00000413345.2:p.Pro38=
ENST00000526579.5:n.178-1059A>T
ENST00000527116.5:n.372A>T
ENST00000528555.5:c.750A>T	ENSP00000435122.1:p.Pro250=
ENST00000530330.1:n.346A>T
ENST00000530356.5:c.750A>T	ENSP00000432307.1:p.Pro250=
ENST00000533318.5:n.970A>T
ENST00000534726.5:c.330A>T	ENSP00000433699.1:p.Pro110=
NM_001301089.1:c.750A>T	NP_001288018.1:p.Pro250=
NM_014758.2:c.2610A>T	NP_055573.2:p.Pro870=
XM_005271546.3:c.2574-1059A>T	XP_005271603.1:n.2574-1059A>T
XM_011542819.1:c.2856A>T	XP_011541121.1:p.Pro952=
XM_011542820.1:c.2844A>T	XP_011541122.1:p.Pro948=
XM_011542821.1:c.2736A>T	XP_011541123.1:p.Pro912=
XM_011542824.1:c.1974A>T	XP_011541126.1:p.Pro658=
XM_011542825.1:c.1131A>T	XP_011541127.1:p.Pro377=
XM_011542826.1:c.996A>T	XP_011541128.1:p.Pro332=
XM_011542827.1:c.876A>T	XP_011541129.1:p.Pro292=
NM_001347918.1:c.2490A>T	NP_001334847.1:p.Pro830=
NM_001347919.1:c.2574-1059A>T	NP_001334848.1:n.2574-1059A>T
NM_001347922.1:c.939A>T	NP_001334851.1:p.Pro313=
NM_001347923.1:c.885A>T	NP_001334852.1:p.Pro295=
NM_001347924.1:c.630A>T	NP_001334853.1:p.Pro210=
NM_001347925.1:c.576A>T	NP_001334854.1:p.Pro192=
NM_001347926.1:c.714-1059A>T	NP_001334855.1:n.714-1059A>T
NM_001347927.1:c.330A>T	NP_001334856.1:p.Pro110=
NR_144939.1:n.3243A>T
XM_011542820.2:c.2844A>T	XP_011541122.1:p.Pro948=
XM_011542821.3:c.2736A>T	XP_011541123.1:p.Pro912=
XM_011542824.2:c.1974A>T	XP_011541126.1:p.Pro658=
XM_011542825.2:c.1131A>T	XP_011541127.1:p.Pro377=
XM_011542826.2:c.996A>T	XP_011541128.1:p.Pro332=
XM_024448521.1:c.2856A>T	XP_024304289.1:p.Pro952=
XR_001747870.1:n.3681A>T
XR_001747872.1:n.3027A>T
XR_001747873.1:n.3341A>T
NM_001301089.2:c.750A>T	NP_001288018.1:p.Pro250=
NM_001347918.2:c.2490A>T	NP_001334847.2:p.Pro830=
NM_001347919.2:c.2574-1059A>T	NP_001334848.2:n.2574-1059A>T
NM_001347920.2:c.*21006A>T	NP_001334849.2:n.*21006A>T
NM_001347922.2:c.939A>T	NP_001334851.2:p.Pro313=
NM_001347923.2:c.885A>T	NP_001334852.2:p.Pro295=
NM_001347924.2:c.630A>T	NP_001334853.1:p.Pro210=
NM_001347925.2:c.576A>T	NP_001334854.1:p.Pro192=
NM_001347926.2:c.714-1059A>T	NP_001334855.1:n.714-1059A>T
NM_001347927.2:c.330A>T	NP_001334856.1:p.Pro110=
NM_014758.3:c.2610A>T MANE Select	NP_055573.3:p.Pro870=
NR_144939.2:n.3235A>T